"Ambry Genetics"[submitter] AND "UBE2U"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330585	NM_001366232.2(UBE2U):c.67G>A (p.Gly23Ser)	UBE2U (G23S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258593	NM_001366232.2(UBE2U):c.85G>A (p.Val29Ile)	UBE2U (V29I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330586	NM_001366232.2(UBE2U):c.250C>T (p.His84Tyr)	UBE2U (H83Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185574	NM_001366232.2(UBE2U):c.362T>A (p.Leu121Gln)	UBE2U (L120Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555380	NM_001366232.2(UBE2U):c.408T>G (p.Asp136Glu)	UBE2U (D136E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239249	NM_001366232.2(UBE2U):c.446G>A (p.Arg149Lys)	UBE2U (R148K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347443	NM_001366232.2(UBE2U):c.490C>T (p.Pro164Ser)	UBE2U (P164S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2603943	NM_001366232.2(UBE2U):c.500G>A (p.Cys167Tyr)	UBE2U (C166Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3330588	NM_001366232.2(UBE2U):c.527T>A (p.Phe176Tyr)	UBE2U (F175Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3330587	NM_001366232.2(UBE2U):c.572C>G (p.Ala191Gly)	UBE2U (A191G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3185575	NM_001366232.2(UBE2U):c.648T>A (p.Asp216Glu)	UBE2U (D215E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign